Cas 1176200-92-2,(S)-N-[[3-[6-[4-[2-(4-methylbenzamido)acetyl]piperazin-1-yl]pyridine-3-yl]-2-oxo-5-oxazolidinyl]methyl]acetamide

1176200-92-2

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Basic information

Product Name: (S)-N-[[3-[6-[4-[2-(4-methylbenzamido)acetyl]piperazin-1-yl]pyridine-3-yl]-2-oxo-5-oxazolidinyl]methyl]acetamide
Synonyms:
CAS NO:1176200-92-2
Molecular Formula:
Molecular Weight: 494.55
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S)-N-[[3-[6-[4-[2-(4-methylbenzamido)acetyl]piperazin-1-yl]pyridine-3-yl]-2-oxo-5-oxazolidinyl]methyl]acetamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-[[3-[6-[4-[2-(4-methylbenzamido)acetyl]piperazin-1-yl]pyridine-3-yl]-2-oxo-5-oxazolidinyl]methyl]acetamide(1176200-92-2)
EPA Substance Registry System: (S)-N-[[3-[6-[4-[2-(4-methylbenzamido)acetyl]piperazin-1-yl]pyridine-3-yl]-2-oxo-5-oxazolidinyl]methyl]acetamide(1176200-92-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1176200-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1176200-92-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,6,2,0 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1176200-92:
(9*1)+(8*1)+(7*7)+(6*6)+(5*2)+(4*0)+(3*0)+(2*9)+(1*2)=132
132 % 10 = 2
So 1176200-92-2 is a valid CAS Registry Number.

1176200-92-2Upstream product

27115-50-0 N-(4-methylbenzoyl)glycine

1176200-92-2Downstream Products

1176200-92-2Relevant academic research and scientific papers

Synthesis and antibacterial activities of eperezolid analogs with glycinyl substitutions

Wang, Xiao-Jun,Wu, Ning,Du, Guang-Jian,Zhao, Shuang-Qi,Yan, Ming,Gu, Lian-Quan

experimental part, p. 377 - 385 (2009/10/23)

A series of eperezolid analogs with glycinyl substitutions were prepared and their antibacterial activities were studied against a panel of susceptible and resistant Gram-positive bacteria. The compounds with N-arylacyl or N-heteroarylacyl glycinyl struct

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